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Treatment of Fanconi anemia patients using fludarabine and low-dose TBI, followed by unrelated donor hematopoietic cell transplantation.

机译:使用氟达拉滨和低剂量TBI治疗Fanconi贫血患者,然后进行无关的供体造血细胞移植。

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摘要

A nonmyeloablative conditioning regimen consisting of fludarabine (FLU) and 2 Gy TBI has been used extensively and with substantial engraftment success without promoting excessive nonrelapse mortality in medically infirm patients requiring hematopoietic cell transplantation. In this paper, we studied this same low-toxicity regimen as a means of promoting engraftment of unrelated donor hematopoietic cell transplantation in patients with Fanconi anemia (FA). All patients tolerated the regimen well with no mucositis or other severe toxicities. Of six patients transplanted, five achieved stable mixed or full donor chimerism. Acute and chronic GVHD occurred in four and three patients, respectively. Three patients are alive and well at a median of 45.9 (range, 20.9-68.1) months after transplant. In summary, this FLU-based regimen facilitates stable engraftment of unrelated PBSCs, but is associated with significant chronic GVHD.
机译:由氟达拉滨(FLU)和2 Gy TBI组成的非清髓性调理方案已被广泛使用,并且在成功植入体内而又不增加需要造血细胞移植的体弱多病患者的非复发死亡率的情况下。在本文中,我们研究了相同的低毒方案,作为促进Fanconi贫血(FA)患者移植无关的供体造血细胞移植的方法。所有患者对方案均耐受良好,无粘膜炎或其他严重毒性反应。在移植的6例患者中,有5例达到了稳定的混合或完全供体嵌合。急性和慢性GVHD分别发生在四名和三名患者中。 3例患者存活并且在移植后的中位数为45.9(范围为20.9-68.1)个月。综上所述,这种基于FLU的方案有助于稳定移植无关的PBSC,但与明显的慢性GVHD有关。

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